# Regulation of CSE-Derived Hydrogen Sulfide in the Heart

> **NIH NIH R01** · EMORY UNIVERSITY · 2024 · $514,162

## Abstract

Project Summary
Hydrogen sulfide (H2S) is an endogenously produced signaling molecule that impacts protein function by
modifying cysteine residues through the formation of a persulfide bond by a process termed sulfhydration
(persulfidation). It is produced enzymatically by three enzymes in the cysteine biosynthesis pathway:
cystathionine-γ-lyase (CSE), cystathionine-β-synthase (CBS), and 3-mercaptopyruvate sulfutransferase (3-
MST). Numerous studies have reported a protective role for H2S in experimental models of acute myocardial
ischemia-reperfusion injury and heart failure. While these studies and others have established a cytoprotective
role for H2S, there are still unresolved questions regarding the biology of H2S. For instance, there is a lack of
understanding in how the endogenous production of H2S is regulated. Additionally, there is a need to identify
protein targets of H2S in response to different stimuli to unravel the mechanism by with H2S impacts adaptation
to stress. This proposal aims to offer new insights into the regulation of the H2S-producing activity of CSE. We
present new data that AMP-activated protein kinase (AMPK) increases CSE-derived H2S production via
phosphorylation of serine 126. Further studies identified perilipin 5 (Plin5) – a protein that promotes the
association of lipid droplets with mitochondria - as a protein modified by sulfhydration following nutrient
deprivation and AMPK activation. Our data also shows that the interaction of lipid droplets with mitochondria
following nutrient deprivation is dependent on CSE. Based on this evidence, we hypothesize that in response
to nutrient stress, AMPK induces the H2S-producing activity of CSE to impart adaptive cellular mechanisms.
Specifically, we hypothesize that CSE-derived H2S maintains energy metabolism during nutrient stress by
regulating the mobilization of lipid droplets to the mitochondria, in part, by altering the sulfhydration of Plin5. In
Aim 1, we will investigate the impact of serine 126 phosphorylation on the H2S-producing activity of CSE. In
Aim 2, we will investigate the Impact of CSE-derived H2S on maintaining Lipid Droplet-fueled β-oxidation
during nutrient deprivation. In Aim 3, we will determine the impact of sulfhydration on Plin5 during nutrient
deprivation. This project breaks new ground in defining a mechanism by which the H2S-producing activity of
CSE is regulated. As such, it has the potential to lead to the development of novel therapies aimed at
harnessing the physiological effects of H2S to combat cardiovascular disease.

## Key facts

- **NIH application ID:** 10818460
- **Project number:** 5R01HL164806-02
- **Recipient organization:** EMORY UNIVERSITY
- **Principal Investigator:** John Winter Calvert
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $514,162
- **Award type:** 5
- **Project period:** 2023-04-01 → 2027-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10818460

## Citation

> US National Institutes of Health, RePORTER application 10818460, Regulation of CSE-Derived Hydrogen Sulfide in the Heart (5R01HL164806-02). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/10818460. Licensed CC0.

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